About the Company :
The firm have more than 10000+ employees and is founded in 1876 and have offices more than 18 countries. The firm have head quarters in Indiana polis. The firm have more than 145 year of excellence and have expert medical professionals with the core values in integrity, excellence and respect for people. During the pandemic times it involved in delivering Covid medicines. The firm have a Nobel prize awarded at 1928 with the liver extract for anemia. The company have many block buster molecules like Cymbalta and have scope of large and small molecular development. The firm have oncology division specialized in delivering world class medicines.
About the Job
Location : Bengaluru
Experience : minimum of 10 years experience in GMP pharma industry
Education : Bachelors in Science or Pharmacy
Required to review the documents archive retrieve and update documentation as per regulatory compliance
Able to plan coordinate for reserves samples and manage the activity
Preparation of regulatory audits and compliance related to the department and handling the same
Required to support in regulatory audits and compliance
Able to participate and lead performance with the Employees 131 and connect repair performance cheque on employees progress to achieve the objectives and offer support to remove barriers and revisit their performance Or the expectations
Daily monitoring of kinetic Temperature report and sample area temperatures
Handling of document oscillation and Running sample reserve management activity
Able to create rest Trust opportunity for employee development in pursuit of purpose and Demonstrating the core values like courage, collaboration, preservance and passion
Ensure that all the team members are compliance with the programmes and policies As well as procedures
Capable to utilise the relationship The relationships of employees and handle the team Further continuous improving leadership capabilities to achieve big goal